9H-fluoren-9-ylmethyl N-[[(2S,3S,5R)-5-(6-benzamidopurin-9-yl)-2-[[(4-methoxyphenyl)-diphenylmethoxy]methyl]oxolan-3-yl]carbamothioyl]carbamate | 556826-41-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• 英文名称: 9H-fluoren-9-ylmethyl N-[[(2S,3S,5R)-5-(6-benzamidopurin-9-yl)-2-[[(4-methoxyphenyl)-diphenylmethoxy]methyl]oxolan-3-yl]carbamothioyl]carbamate
• CAS: 556826-41-6
• 化学式: C₅₃H₄₅N₇O₆S
• 分子量: 908.05
• InChiKey: MRDCMGPASUGELE-VURFOUDESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.1
• 重原子数：
  67
• 可旋转键数：
  14
• 环数：
  10.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  183
• 氢给体数：
  3
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  5'-monomethoxytritylamino-3'-(N'-9-fluorenylmethoxycarbonylthiouria)-2',3',5'-trideoxythymidine 、 、 9H-fluoren-9-ylmethyl N-[[(2S,3S,5R)-5-(6-benzamidopurin-9-yl)-2-[[(4-methoxyphenyl)-diphenylmethoxy]methyl]oxolan-3-yl]carbamothioyl]carbamate 、 9H-fluoren-9-ylmethyl N-[[(2R,3S,5R)-5-(6-benzamidopurin-9-yl)-2-[[[(4-methoxyphenyl)-diphenylmethyl]amino]methyl]oxolan-3-yl]carbamothioyl]carbamate 生成
  参考文献：
  名称：

  Solid-Phase synthesis of positively charged deoxynucleic guanidine (DNG) oligonucleotide mixed sequences

  摘要：

  Positively charged DNG oligonucleotide mixed sequences containing A/T bases were prepared by solid-phase synthesis. Synthesis proceeds in 3'-->5' direction and involves coupling of 3'-Fmoc protected thiourea in the presence of HgCl2/TEA with the corresponding 5'-amine of the growing oligo chain. DNG binding characteristics with complementary DNA and with itself have been evaluated. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00119-7
• 作为产物：
  描述：

  5-叠氮基-5-脱氧胸腺嘧啶脱氧核苷 在 palladium on activated charcoal 吡啶 、 4-二甲氨基吡啶 、 叠氮化锂 、 氢气 、 N,N'-二环己基碳二亚胺 作用下， 以 1,4-二氧六环 、 乙醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 39.0h， 生成 9H-fluoren-9-ylmethyl N-[[(2S,3S,5R)-5-(6-benzamidopurin-9-yl)-2-[[(4-methoxyphenyl)-diphenylmethoxy]methyl]oxolan-3-yl]carbamothioyl]carbamate
  参考文献：
  名称：

  Solid-Phase synthesis of positively charged deoxynucleic guanidine (DNG) oligonucleotide mixed sequences

  摘要：

  Positively charged DNG oligonucleotide mixed sequences containing A/T bases were prepared by solid-phase synthesis. Synthesis proceeds in 3'-->5' direction and involves coupling of 3'-Fmoc protected thiourea in the presence of HgCl2/TEA with the corresponding 5'-amine of the growing oligo chain. DNG binding characteristics with complementary DNA and with itself have been evaluated. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00119-7